Canonical Allele Identifier: CA2298481275
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477761G= , CM000680.2:g.41477761G= GRCh38
NC_000018.9:g.39057725G= , CM000680.1:g.39057725G= GRCh37
NC_000018.8:g.37311723G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26373G=